Compatibility study between ibuproxam and pharmaceutical excipients using differential scanning calorimetry, hot-stage microscopy and scanning electron microscopy

Differential scanning calorimetry (DSC) was used as a screening technique for assessing the compatibility of ibuproxam with some currently employed pharmaceutical excipients. The influence of processing effects (simple blending, cogrinding or kneading) on drug stability was also evaluated. On the ba...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 1998-10, Vol.18 (1-2), p.151-163
Hauptverfasser: Mura, P., Faucci, M.T., Manderioli, A., Bramanti, G., Ceccarelli, L.
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container_end_page 163
container_issue 1-2
container_start_page 151
container_title Journal of pharmaceutical and biomedical analysis
container_volume 18
creator Mura, P.
Faucci, M.T.
Manderioli, A.
Bramanti, G.
Ceccarelli, L.
description Differential scanning calorimetry (DSC) was used as a screening technique for assessing the compatibility of ibuproxam with some currently employed pharmaceutical excipients. The influence of processing effects (simple blending, cogrinding or kneading) on drug stability was also evaluated. On the basis of DSC results, ibuproxam was found to be compatible with corn starch, avicel and sodium carboxymethylcellulose. Some drug-excipient interaction was observed with polyethyleneglycol 4000, palmitic acid, stearic acid, Ca and Mg stearate. Actual solid-phase interactions of the drug with polyvinylpolypyrrolidone and polyvinylpirrolidone K30 were induced by mechanical treatments. Hot-stage microscopy (HSM) and scanning electron microscopy (SEM) were of help in interpreting the DSC results and excluding in all cases relevant pharmaceutical incompatibilities.
doi_str_mv 10.1016/S0731-7085(98)00171-X
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The influence of processing effects (simple blending, cogrinding or kneading) on drug stability was also evaluated. On the basis of DSC results, ibuproxam was found to be compatible with corn starch, avicel and sodium carboxymethylcellulose. Some drug-excipient interaction was observed with polyethyleneglycol 4000, palmitic acid, stearic acid, Ca and Mg stearate. Actual solid-phase interactions of the drug with polyvinylpolypyrrolidone and polyvinylpirrolidone K30 were induced by mechanical treatments. Hot-stage microscopy (HSM) and scanning electron microscopy (SEM) were of help in interpreting the DSC results and excluding in all cases relevant pharmaceutical incompatibilities.</description><subject>Benzeneacetamides</subject><subject>Biological and medical sciences</subject><subject>Bones, joints and connective tissue. Antiinflammatory agents</subject><subject>Calorimetry, Differential Scanning</subject><subject>Compatibility</subject><subject>Differential scanning calorimetry</subject><subject>Drug Incompatibility</subject><subject>Drug Stability</subject><subject>Excipients</subject><subject>Excipients - chemistry</subject><subject>Hot Temperature - adverse effects</subject><subject>Hot-stage microscopy</subject><subject>Hydroxamic Acids - chemistry</subject><subject>Ibuproxam</subject><subject>Medical sciences</subject><subject>Microscopy</subject><subject>Microscopy, Electron, Scanning</subject><subject>Pharmacology. 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Antiinflammatory agents</topic><topic>Calorimetry, Differential Scanning</topic><topic>Compatibility</topic><topic>Differential scanning calorimetry</topic><topic>Drug Incompatibility</topic><topic>Drug Stability</topic><topic>Excipients</topic><topic>Excipients - chemistry</topic><topic>Hot Temperature - adverse effects</topic><topic>Hot-stage microscopy</topic><topic>Hydroxamic Acids - chemistry</topic><topic>Ibuproxam</topic><topic>Medical sciences</topic><topic>Microscopy</topic><topic>Microscopy, Electron, Scanning</topic><topic>Pharmacology. 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The influence of processing effects (simple blending, cogrinding or kneading) on drug stability was also evaluated. On the basis of DSC results, ibuproxam was found to be compatible with corn starch, avicel and sodium carboxymethylcellulose. Some drug-excipient interaction was observed with polyethyleneglycol 4000, palmitic acid, stearic acid, Ca and Mg stearate. Actual solid-phase interactions of the drug with polyvinylpolypyrrolidone and polyvinylpirrolidone K30 were induced by mechanical treatments. Hot-stage microscopy (HSM) and scanning electron microscopy (SEM) were of help in interpreting the DSC results and excluding in all cases relevant pharmaceutical incompatibilities.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>9863953</pmid><doi>10.1016/S0731-7085(98)00171-X</doi><tpages>13</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Benzeneacetamides
Biological and medical sciences
Bones, joints and connective tissue. Antiinflammatory agents
Calorimetry, Differential Scanning
Compatibility
Differential scanning calorimetry
Drug Incompatibility
Drug Stability
Excipients
Excipients - chemistry
Hot Temperature - adverse effects
Hot-stage microscopy
Hydroxamic Acids - chemistry
Ibuproxam
Medical sciences
Microscopy
Microscopy, Electron, Scanning
Pharmacology. Drug treatments
Scanning electron microscopy
title Compatibility study between ibuproxam and pharmaceutical excipients using differential scanning calorimetry, hot-stage microscopy and scanning electron microscopy
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